Neuroimaging Research Unit, Institute of Experimental Neurology, Division of Neuroscience, Ospedale San Raffaele, Milan, Italy.
Neurobiol Aging. 2012 Jun;33(6):1023-33. doi: 10.1016/j.neurobiolaging.2010.09.021. Epub 2010 Nov 12.
We investigated patterns of white matter (WM) loss in 18 early onset (EO) and 24 late onset (LO) Alzheimer's disease (AD) patients compared with 42 healthy controls (HC), and explored relationships of WM atrophy and apolipoprotein E (ApoE) genotype. Subjects underwent magnetic resonance imaging (MRI). Patterns of WM were assessed using voxel-based morphometry. Compared with healthy controls, LOAD patients had a selective parahippocampal WM loss, while EOAD patients experienced a more widespread pattern of posterior WM atrophy. The distinct regional distribution of WM atrophy reflected the topography of gray matter (GM) loss. ApoE ε4 status was associated with a greater parahippocampal WM loss in both AD groups. The greater WM atrophy in EOAD than LOAD fits with the evidence that EOAD is a more aggressive form of the disease. The ApoE ε4 effect on WM damage in AD is restricted to specific WM regions and does not seem to be related to age of onset.
我们研究了 18 例早发性(EO)和 24 例晚发性(LO)阿尔茨海默病(AD)患者与 42 名健康对照(HC)之间的白质(WM)丢失模式,并探讨了 WM 萎缩与载脂蛋白 E(ApoE)基因型的关系。受试者接受了磁共振成像(MRI)检查。采用基于体素的形态测量法评估 WM 模式。与健康对照组相比,LOAD 患者存在选择性海马旁 WM 丢失,而 EOAD 患者则存在更广泛的后部 WM 萎缩。WM 萎缩的不同区域分布反映了灰质(GM)丢失的分布。ApoE ε4 状态与 AD 两组患者的海马旁 WM 丢失增多有关。EOAD 患者 WM 萎缩程度大于 LOAD,这与 EOAD 是一种侵袭性更强的疾病的证据一致。ApoE ε4 对 AD 患者 WM 损伤的影响仅限于特定的 WM 区域,似乎与发病年龄无关。